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FDA Inspection
•Gemini Pharmaceuticals, Inc.•March 23, 2010

Gemini Pharmaceuticals, Inc. – FDA Inspection, Mar 23, 2010

Record Details

This FDA Inspection record concerns Gemini Pharmaceuticals, Inc., with an inspection on March 23, 2010, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Gemini Pharmaceuticals, Inc.
Inspection Date
March 23, 2010
Product Type
Veterinary
Office
Center for Veterinary Medicine
View Company Profile

ID · 6d0414fa-9cc5-4ace-973e-a5c2f96983bb

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
652318
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

FDA Citations

2
  1. 21 CFR 211.68(b)Computer control of master formula records
  2. 21 CFR 211.68(b)Backup file not maintained

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Gemini Pharmaceuticals, Inc.

9
DateClassificationOfficeProject area
May 15, 2026VAINew York District OfficeFood Composition, Standards, Labeling and Econ
July 26, 2022VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 23, 2018NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
February 16, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 30, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for Gemini Pharmaceuticals, Inc.
  • FDA Inspection 1317530 - 2026-05-15
  • FDA Inspection 1175407 - 2022-07-26
  • FDA Inspection 1064447 - 2018-08-23
  • FDA Inspection 1041525 - 2018-02-16
  • FDA Inspection 936886 - 2015-06-30

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